Neurodegeneration, infantile-onset, biotin-responsive

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Subtype of: Neurodegeneration
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodegeneration, infantile-onset, biotin-responsive
MONDO_0033546
SLC5A6 Causal
29669219 27904971 31754459 31392107 23104561 35013551
Open Targets
All1 Causal1 Unknown0
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Sodium-dependent multivitamin transporter deficiency 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Peripheral motor neuropathy, childhood-onset, biotin-responsive 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Genetic neurodegenerative disease 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Uterine fibroid 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Neurodevelopmental disorder 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6.